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临床试验/NCT03757299
NCT03757299已完成不适用

Promoting Comprehensive Cervical Cancer Prevention and Better Women Health in Cameroon

Prof. Patrick Petignat2 个研究点 分布在 1 个国家目标入组 4,473 人开始时间: 2018年10月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
4,473
试验地点
2
主要终点
Sensitivity and specificity of HPV test followed by VIA/VILI to detect cervical precancerous lesions in sub-Saharan Africa using histology as gold standard

研究概览

简要总结

In sub-Saharan Africa, cervical cancer is the leading cause of cancer death among women because of the difficulty in implementing screening programs. The main obstacles in these countries are poverty, lack of healthcare infrastructures and trained practitioners. With the availability of new technologies, researchers are looking for new strategies adapted to low- and middle-income countries to identify cervical precancerous lesions.

Current evidence shows that Human Papilloma Virus (HPV) testing is more effective than cytology (Pap smear) for cervical cancer screening in resource-limited settings. Indeed, the GeneXpert® HPV test offers the opportunity to prevent cervical cancer (CC) in a single visit: rapid detection of high-risk HPV (HPV) infection followed by same day treatment of HPV-positive women during the same visit (screen-and-treat approach).

However only a small proportion of HPV-positive women will develop cervical (pre)cancer, making it important to select those to treat. This triage can be achieved by colposcopy, cytology and visual inspection after application of acetic acid (VIA). Though VIA is the triage test recommended by WHO for resource-limited countries, it has not yet been widely assessed in sub-Saharan Africa (SSA).

The main objective of the investigators is to assess the performance of HPV-test followed by Visual Inspection after application of Acetic acid and Lugol's iodine VIA/VILI to detect cervical precancerous lesions in a screen-and-treat strategy in Cameroon (sub-Saharan Africa) where there is no cervical cancer-screening program.

The investigators organized a successful free screening campaign in Cameroon in 2015 that allowed to identify the expectations of women and their eagerness to benefit from prevention of gynecological cancers and sexually transmitted diseases.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
30 Years 至 49 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Women aged 30-49 years, able to comply with the study protocol

排除标准

  • Pregnancy
  • Previous total hysterectomy
  • Conditions impairing examination of the cervix

结局指标

主要结局

Sensitivity and specificity of HPV test followed by VIA/VILI to detect cervical precancerous lesions in sub-Saharan Africa using histology as gold standard

时间窗: 3 - 5 years

VIA/VILI is assessed by pelvic examination and Sensitivity and specificity are measured by using histology as gold stantard

次要结局

  • Provide teaching material for professional training on cervical cancer prevention through VIA/VILI (cervical images database)(3 - 5 years)
  • Acceptability rate of self-HPV test and cervical cancer screening procedures(3 years)
  • Thermal ablation efficacy rate(3 - 5 years)
  • Sexual dysfunction score, score of anxiety and method of contraception after screening procedures,(2 years)
  • VIA test-positive rate after 1- year follow-up of VIA-negative tests(3 - 5 years)
  • Increase awareness on gynecological pathologies, including cervical cancer, sexually transmitted diseases and HIV, vaginal fistula in the community of the study area,(3-5 years)
  • Prevalence of HPV infection(3 - 5 years)
  • Prevalence of cervical pre-cancer and cancer among Cameroonian women(3 - 5 years)
  • Proportion of side effects and complications after thermoablation or LEEP(3 - 5 years)
  • Acceptability rate of thermoablation(3 years)
  • Number of women screened with and without community health care workers.(2 years)
  • HPV clearance(3 - 5 years)
  • Persistance of CIN2+ disease at the 12-month follow-up(3 - 5 years)
  • VIA test-positive rate (HPV-positive women);(3 - 5 years)

研究者

发起方
Prof. Patrick Petignat
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Prof. Patrick Petignat

Director of the gynecology departement

University Hospital, Geneva

研究点 (2)

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